Mittal Manish, Lele Pushkar P, Kaler Eric W, Furst Eric M
Department of Chemical Engineering and Center for Molecular and Engineering Thermodynamics, University of Delaware, 150 Academy Street, Newark, Delaware 19716, USA.
J Chem Phys. 2008 Aug 14;129(6):064513. doi: 10.1063/1.2969103.
Micrometer-sized polystyrene particles form two-dimensional crystals in alternating current (ac) electric fields. The induced dipole-dipole interaction is the dominant force that drives this assembly. We report measurements of forces between colloidal particles in ac electric fields using optical tweezers and find good agreement with the point dipole model. The magnitude of the pair interaction forces depends strongly on the bulk solution conductivity and decreases as the ionic strength increases. The forces also decrease with increasing field frequency. The salt and frequency dependences are consistent with double layer polarization with a characteristic relaxation frequency omega(CD) approximately a(2)/D, where a is the particle radius and D is the ion diffusivity. This enables us to reinterpret the order-disorder transition reported for micrometer-sized polystyrene particles [Lumsdon et al., Langmuir 20, 2108 (2004)], including the dependence on particle size, frequency, and ionic strength. These results provide a rational framework for identifying assembly conditions of colloidal particles in ac fields over a wide range of parameters.
微米级聚苯乙烯颗粒在交变电场中形成二维晶体。感应偶极 - 偶极相互作用是驱动这种组装的主导力。我们报告了使用光镊测量交变电场中胶体颗粒间力的结果,并发现与点偶极模型吻合良好。成对相互作用力的大小强烈依赖于本体溶液的电导率,且随离子强度增加而减小。这些力也随场频率增加而减小。盐和频率的依赖性与具有特征弛豫频率ω(CD)≈a(2)/D的双层极化一致,其中a是颗粒半径,D是离子扩散率。这使我们能够重新解释微米级聚苯乙烯颗粒所报道的有序 - 无序转变[Lumsdon等人,《朗缪尔》20, 2108 (2004)],包括对颗粒尺寸、频率和离子强度的依赖性。这些结果为确定在广泛参数范围内交变场中胶体颗粒的组装条件提供了一个合理的框架。